Anser indicusbar-headed goose

Ge­o­graphic Range

Bar-headed geese (Anser in­di­cus) have a breed­ing range that stretches from Mon­go­lia south through Rus­sia and West­ern China to Tibet and as far west as Kyr­gyzs­tan. Ap­prox­i­mately 25% of the global pop­u­la­tion of bar-headed geese win­ter on the south­ern Ti­betan-Qing­hai Plateau. An­other win­ter­ing area for a por­tion of the pop­u­la­tion is India and Bangladesh. (Guo-Gang, et al., 2011; Takekawa, et al., 2009)

Habi­tat

Bar-headed geese can be found at high el­e­va­tions. They use habi­tats like moun­tain grass­lands and crop fields from sur­round­ing vil­lages. Bar-headed geese tend to use fresh­wa­ter marshes, lakes, and streams that are around el­e­va­tions of 4,000 to 6,000 me­ters above sea level as stop-over and over-win­ter­ing sites. Some geese have even been re­ported to mi­grate at al­ti­tudes of 9,000 me­ters when they cross the Hi­malaya Moun­tains. (Guo-Gang, et al., 2011; Mid­dle­ton, 1992; Scott, et al., 2009; Takekawa, et al., 2009)

  • Range elevation
    Sea Level to 6,000 m
    to ft

Phys­i­cal De­scrip­tion

Bar-headed geese have grey bod­ies, with or­ange legs and a black and white neck. This species is named for the ob­vi­ous black U-shaped bars on the back of the white head. They weigh be­tween 2 and 3 kg (4.5 and 6.5 lbs) with a wingspan be­tween 140 and 160 cm (55 and 62 inch), and are be­tween 68 and 78 cm (27 and 30 inch) in length. Bar-headed geese have a basal meta­bolic rate of 756 cubic cen­time­ters of oxy­gen per hour. (Tam­melin, 2012; Ward, et al., 2002)

  • Sexual Dimorphism
  • sexes alike
  • Range mass
    2.0 to 3.0 kg
    4.41 to 6.61 lb
  • Range length
    68 to 78 cm
    26.77 to 30.71 in
  • Range wingspan
    140 to 160 cm
    55.12 to 62.99 in
  • Average basal metabolic rate
    756 cm3.O2/g/hr

Re­pro­duc­tion

Bar-headed geese are sea­sonal breed­ers. They ex­hibit a monog­a­mous mat­ing sys­tem, where males pair with one sin­gle fe­male for sev­eral years. Dur­ing times when the pop­u­la­tion is bi­ased to­wards fe­males a polyg­y­nous sys­tem is adopted where a monog­a­mous pair may be joined by mul­ti­ple sec­ondary fe­males. These sec­ondary fe­males also breed with the male of the pair. Be­cause they breed in large colonies, fe­males de­fend their nests from so­cially lower fe­males that may be using brood par­a­sitism to in­crease the likely hood of their off­spring's sur­vival. (Lam­precht, 1987)

Bar-headed geese typ­i­cally breed on an an­nual basis. This oc­curs dur­ing the spring. Nest­ing oc­curs from the last week of April until June. They typ­i­cally lay 3 to 8 eggs on av­er­age. After 28 to 30 days the goslings hatch. There was lit­tle in­for­ma­tion on the birth mass of the goslings. They then fledge by 55 to 60 days, and reach sex­ual ma­tu­rity at 3 years of age. Bar-headed geese tend to breed on the Ti­betan-Qing­hai Plateau. They lay their eggs in ground nests at high el­e­va­tions in the high­land marshes and lakes. (Prins and van Wieren, 2004; Takekawa, et al., 2009)

  • Breeding interval
    Bar-headed geese breed annually (once yearly).
  • Breeding season
    Bar-headed geese breed in the last week of April through July.
  • Range eggs per season
    3 to 8
  • Range time to hatching
    28 to 30 days
  • Range fledging age
    55 to 60 days
  • Range time to independence
    55 to 60 days
  • Average age at sexual or reproductive maturity (female)
    3 years
  • Average age at sexual or reproductive maturity (male)
    3 years

Bar-headed geese use bi­parental care when rais­ing young. Stud­ies show that male bar-headed geese are more alert and de­fen­sive when in the pres­ence of their goslings. These same stud­ies show that the goslings have the added ben­e­fit of an in­creased sur­vival rate from hav­ing both par­ents. Both par­ents pro­vide their goslings with pro­tec­tion from preda­tors and other geese. In ad­di­tion to that the par­ents also pro­tect the goslings' food. (Friedl, 1993; Schnei­der and Lam­precht, 1990)

Lifes­pan/Longevity

Lit­tle in­for­ma­tion is pub­lished on the lifes­pan of bar-headed geese. Like most geese they are long-lived. A close rel­a­tive, grey­lag geese, have a lifes­pan of 20 years in the wild and the old­est one in cap­tiv­ity lived 31 years. (de Ma­g­a­l­haes and Costa, 2009; de Ma­g­a­l­haes and Costa, 2009)

  • Average lifespan
    Status: wild
    20 years
  • Average lifespan
    Status: captivity
    20 years

Be­hav­ior

This species is typ­i­cal to most in the order Anser­i­formes in that they are a so­cial species mi­grat­ing in fam­ily groups or large colonies. They are very motile mi­grat­ing twice a year over the Hi­malaya Moun­tains to and from their breed­ing grounds on the Ti­betan-Qing­hai Plateau. They mi­grate in "V"-for­ma­tions or vari­a­tions of it. They have a so­cial hi­er­ar­chy con­sist­ing of mated male-fe­male pairs being the high­est, fol­lowed by sec­ondary fe­males that are usu­ally part of a harem, and low­est so­cially is lone fe­males. This harem usu­ally forms when the pop­u­la­tion is bi­ased to­wards fe­males. Bar-headed geese make ground nests with shal­low de­pres­sions at high el­e­va­tions. They de­fend these nests from preda­tors and from other so­cially lower fe­males. ("Bar-headed geese - the as­tro­nauts among mi­gra­tory birds", 2011; Prins and van Wieren, 2004; Scott, et al., 2009; Speak­man and Banks, 1998)

Home Range

Their Breed­ing range is in West­ern China, Mon­go­lia, and on the Ti­betan-Qing­hai Plateau. Their non-breed­ing range is in India, Bangladesh and Nepal. (Prins and van Wieren, 2004; Schnei­der and Lam­precht, 1990; Scott, et al., 2009; Ward, et al., 2002)

Com­mu­ni­ca­tion and Per­cep­tion

Like most geese, bar-headed geese fly in "V"-shaped for­ma­tions. When the lead bird gets tired they fall to the back of the for­ma­tion and an­other goose takes the lead. The for­ma­tion can vary from a tra­di­tional V to other shapes like "J"-shape and the echeleon shape where one arm of the "V"-shape is miss­ing. The ben­e­fit of this style of flight is that each in­di­vid­ual flies with re­duced drag, which in turn saves them en­ergy. They use vocal com­mu­ni­ca­tions and vi­sual cues to main­tain their spac­ing while fly­ing in these for­ma­tions. This also as­sists them in stay­ing in closely re­lated fam­ily groups as they move from tra­di­tional feed­ing and breed­ing areas. Like other wa­ter­fowl they can also see in the ul­tra­vi­o­let spec­trum of light. (Speak­man and Banks, 1998)

Food Habits

Bar-headed geese gen­er­ally feed on the high­land grasses sur­round­ing their lakes and streams where they nest. Dur­ing other times of the year they can be found eat­ing on agri­cul­tural crops such as corn, wheat, bar­ley, and rice. (Akbar, et al., 2005)

  • Animal Foods
  • fish
  • insects
  • Plant Foods
  • leaves
  • roots and tubers
  • seeds, grains, and nuts

Pre­da­tion

From the air the bar-headed geese are prey for sea ea­gles, golden ea­gles, crows, and ravens. On the ground the geese are preyed upon by red foxes. Some of the adap­ta­tions the geese have de­vel­oped is the abil­ity to sur­vive at high al­ti­tudes. This lim­its the amount of ground preda­tors that can reach them. They can sur­vive at high al­ti­tudes be­cause they have a higher den­sity of cap­il­lar­ies that are spaced closer to­gether this al­lows them to de­liver more oxy­gen to their mus­cles, in par­tic­u­lar their flight mus­cles. In ad­di­tion to their cap­il­lar­ies they also have he­mo­glo­bin in their blood that is more ef­fi­cient at tak­ing in oxy­gen. An­other adap­ta­tion is that these geese tend to live in large colonies or smaller fam­ily groups which en­hances preda­tor de­tec­tion. (Prins and van Wieren, 2004; Scott, et al., 2009)

Ecosys­tem Roles

These geese are prey for an­i­mals such as red foxes, and golden ea­gles. Some can also be par­a­sites by using higher ranked fe­males as hosts to raise their off­spring. In ad­di­tion they are also car­ri­ers of the H5N1 virus and ca­pa­ble of pass­ing the virus to hu­mans, and other an­i­mals as well. They as­sist in the dis­per­sal of grass seeds they eat through­out the year. (Cui, et al., 2011; Prins and van Wieren, 2004; Weigmann and Lam­precht, 1991)

  • Ecosystem Impact
  • disperses seeds

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

These geese ben­e­fit hu­mans be­cause of eco­tourism to the wildlife areas that they use as re­fu­el­ing stops dur­ing their mi­gra­tions. "The East Cal­cutta Wet­lands in West­ern Ben­gal (a stop over site for mi­grat­ing Bar-headed Geese) has en­vi­ron­men­tal ben­e­fits worth 38.54 mil­lion dol­lars"(Bhat­tacharyya et al., 2008). (Bhat­tacharyya, et al., 2008)

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

Bar-headed geese were one of the first species to show signs of the H5N1 (Bird Flu) virus. In ad­di­tion to car­ry­ing the virus the geese are also pests to the local vil­lagers. Since they feed on the wheat, rice, and other crops around their roost­ing areas, they can cause dam­age to farm fields. (Cui, et al., 2011)

  • Negative Impacts
  • injures humans
    • carries human disease
  • crop pest

Con­ser­va­tion Sta­tus

Bar-headed geese are listed on the IUCN Red List as Least Con­cerned. They have no spe­cial sta­tus under the US Mi­gra­tory Bird Act or on the US Fed­eral List be­cause there is no pop­u­la­tion liv­ing in the US. Nor are they pro­tected under the US En­dan­gered Species Act. CITES con­tains no spe­cial sta­tus for the species ei­ther. (Butchart and Symes, 2012)

Con­trib­u­tors

Do­minick Cucinello (au­thor), Uni­ver­sity of Wis­con­sin-Stevens Point, Christo­pher Yahnke (ed­i­tor), Uni­ver­sity of Wis­con­sin-Stevens Point, Laura Podzikowski (ed­i­tor), Spe­cial Pro­jects.

Glossary

Palearctic

living in the northern part of the Old World. In otherwords, Europe and Asia and northern Africa.

World Map

acoustic

uses sound to communicate

agricultural

living in landscapes dominated by human agriculture.

bilateral symmetry

having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.

brackish water

areas with salty water, usually in coastal marshes and estuaries.

chemical

uses smells or other chemicals to communicate

colonial

used loosely to describe any group of organisms living together or in close proximity to each other - for example nesting shorebirds that live in large colonies. More specifically refers to a group of organisms in which members act as specialized subunits (a continuous, modular society) - as in clonal organisms.

dominance hierarchies

ranking system or pecking order among members of a long-term social group, where dominance status affects access to resources or mates

ecotourism

humans benefit economically by promoting tourism that focuses on the appreciation of natural areas or animals. Ecotourism implies that there are existing programs that profit from the appreciation of natural areas or animals.

endothermic

animals that use metabolically generated heat to regulate body temperature independently of ambient temperature. Endothermy is a synapomorphy of the Mammalia, although it may have arisen in a (now extinct) synapsid ancestor; the fossil record does not distinguish these possibilities. Convergent in birds.

female parental care

parental care is carried out by females

fertilization

union of egg and spermatozoan

folivore

an animal that mainly eats leaves.

freshwater

mainly lives in water that is not salty.

granivore

an animal that mainly eats seeds

herbivore

An animal that eats mainly plants or parts of plants.

iteroparous

offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).

magnetic

(as perception channel keyword). This animal has a special ability to detect the Earth's magnetic fields.

male parental care

parental care is carried out by males

marsh

marshes are wetland areas often dominated by grasses and reeds.

migratory

makes seasonal movements between breeding and wintering grounds

monogamous

Having one mate at a time.

motile

having the capacity to move from one place to another.

native range

the area in which the animal is naturally found, the region in which it is endemic.

oriental

found in the oriental region of the world. In other words, India and southeast Asia.

World Map

oviparous

reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.

polygynous

having more than one female as a mate at one time

seasonal breeding

breeding is confined to a particular season

sexual

reproduction that includes combining the genetic contribution of two individuals, a male and a female

tactile

uses touch to communicate

temperate

that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).

terrestrial

Living on the ground.

territorial

defends an area within the home range, occupied by a single animals or group of animals of the same species and held through overt defense, display, or advertisement

tropical savanna and grassland

A terrestrial biome. Savannas are grasslands with scattered individual trees that do not form a closed canopy. Extensive savannas are found in parts of subtropical and tropical Africa and South America, and in Australia.

savanna

A grassland with scattered trees or scattered clumps of trees, a type of community intermediate between grassland and forest. See also Tropical savanna and grassland biome.

temperate grassland

A terrestrial biome found in temperate latitudes (>23.5° N or S latitude). Vegetation is made up mostly of grasses, the height and species diversity of which depend largely on the amount of moisture available. Fire and grazing are important in the long-term maintenance of grasslands.

visual

uses sight to communicate

young precocial

young are relatively well-developed when born

Ref­er­ences

2011. "Bar-headed geese - the as­tro­nauts among mi­gra­tory birds" (On-line). Goose.​org. Ac­cessed Au­gust 08, 2012 at http://​www.​goose.​org/​englisch/​bar-headed-goose.​html.

Akbar, M., R. Khan, S. Mehboob, Z. Nisa. 2005. Wildlife of Bor­der Belt Game Re­serve Dis­trict Narowal, Pun­jab, Pak­istan. Pak. j. life soc. sci., 3(1-2): 13-17.

Bhat­tacharyya, A., S. Sen, P. Roy, A. Mazum­dar. 2008. A Crit­i­cal Study on Sta­tus of East Kolkata Wet­lands with Spe­cial Em­pha­sis on Water Birds as Bio-In­di­ca­tor. Pro­ceed­ings of Taal2007: The 12th World Lake Con­fer­ence, 12: 1561-1570.

Butchart, S., A. Symes. 2012. "Anser in­di­cus" (On-line). The IUCN Red List of Threat­ened Species. Ac­cessed Au­gust 06, 2012 at http://​www.​iucnredlist.​org/​details/​full/​100600379/​0.

Cui, P., Y. Hou, a. et.. 2011. Bird Mi­gra­tion and Risk for H5N1 Transs­mis­sion into Qing­hai Lake, China. Vec­tor Bome Zoonotic Dis., 11(5): 567-576. Ac­cessed Au­gust 09, 2012 at http://​www.​ncbi.​nlm.​nih.​gov/​pmc/​articles/​PMC3096498/?​tool=pmcentrez.

Friedl, T. 1993. In­tr­a­clutch Egg-Mass Vari­a­tion in Geese: Mech­a­nism for Brood Re­duc­tion in Pre­co­cial Birds. The Auk, 110(1): 129-132. Ac­cessed Au­gust 09, 2012 at http://​library.​unm.​edu/​sora/​Auk/​v110n01/​p0129-p0132.​pdf.

Guo-Gang, Z., L. Dong-Ping, H. Yun-Qiu, J. Hong-Xing, D. Ming, Q. Fa-Wen, L. Jun, X. Zhi, L. Feng-Shan. 2011. Mi­gra­tion Routes and Stop-Over Sites De­ter­mined with Satel­lite Track­ing of Bar-Headed Geese Anser in­di­cus Breed­ing at Qing­hai Lake, China. Wa­ter­birds, 34(1): 112-116. Ac­cessed Au­gust 05, 2012 at http://​www.​bioone.​org/​doi/​full/​10.​1675/​063.​034.​0115.

Lam­precht, J. 1987. Fe­male Re­pro­duc­tive Strate­gies in Bar-headed Geese (Anser in­di­cus): Why Are Geese Monog­a­mous?. Be­hav­ioral Ecol­ogy and So­cial­bi­ol­ogy, 21(5): 297-305. Ac­cessed Au­gust 06, 2012 at http://​www.​jstor.​org/​stable/​4600095.

Mid­dle­ton, B. 1992. Habi­tat and Food Pref­er­ences of Grey­lag and Bar­headed Geese Win­ter­ing in the Ke­o­ladeo Na­tional Park, India. Jour­nal of Trop­i­cal Ecol­ogy, 8 No.2: 181-193. Ac­cessed Au­gust 05, 2012 at http://​www.​jstor.​org/​stable/​2559700.

Prins, H., S. van Wieren. 2004. Num­ber, pop­u­la­tion struc­ture and habi­tat use of bar-headed geese Aniser in­di­cus in Ladakh (India) dur­ing the brood-rear­ing pe­riod. Acta Zo­o­log­ica Sinica, 50(5): 738-744.

Schnei­der, J., J. Lam­precht. 1990. The im­por­tance of bi­parental care in a pre­coial, monog­a­mous bird, the bar-headed goose (Aniser in­di­cus). Be­hav­ioral Ecol­ogy and So­cial­bi­ol­ogy, 27: 415-419. Ac­cessed Au­gust 07, 2012 at http://​www.​jstor.​org.​ezproxy.​uwsp.​edu/​stable/​pdfplus/​4600500.​pdf.

Scott, G., S. Eggin­ton, J. Richards, W. Mil­som. 2009. Evo­lu­tion of mus­cle phe­no­type for ex­treme high al­ti­tude flight in the bar-headed goose. Proc Biol Sci, 276(1673): 3645-3653.

Speak­man, J., D. Banks. 1998. The func­tion of flight for­ma­tions in Grey­lag Geese Anser anser; en­ergy sav­ing or ori­en­ta­tion?. Ibis, 140: 280-287.

Takekawa, J., S. Heath, D. Dou­glas, W. Perry, Javed Salim, S. New­man. 2009. Ge­o­graphic vari­a­tion in Bar-headed Geese Anser in­di­cus: con­nec­tiv­ity of win­ter­ing areas and breed­ing grounds across a broad front. Wild­fowl, 59: 100-123. Ac­cessed Au­gust 05, 2012 at https://​www.​wwt.​org.​uk/​userfiles/​files/​11_​Takekawa_​pp100_​123.​pdf.

Tam­melin, H. 2012. "Bar-headed Goose" (On-line). Na­ture­Gate. Ac­cessed Au­gust 09, 2012 at http://​www.​luontoportti.​com/​suomi/​en/​tekijat/​.

Ward, S., C. Bishop, A. Woakes, P. But­ler. 2002. Heart rate and the rate of oxy­gen con­sump­tion of fly­ing and walk­ing bar­na­cle geese (Branta leu­cop­sis) and bar-headed geese (Anser in­di­cus). The Jour­nal of Ex­per­i­men­tal Bi­ol­ogy, 205: 3347–3356.

Weigmann, C., J. Lam­precht. 1991. In­traspe­cific nest par­a­sitism in bar-headed geese, Anser in­di­cus. An­i­mal Be­hav­iour, 41: 677-688.

de Ma­g­a­l­haes, J., J. Costa. 2009. A data­base of ver­te­brate longevity records and their re­la­tion to other life-his­tory traits.. Jour­nal of Evo­lu­tion­ary Bi­ol­ogy, 22(8): 1770-1774.